Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | (2-Amino-5-(trifluoromethyl)phenyl)(phenyl)methanone | HCID 13014169 | — |
| Reactant | HCID 178525261 | HCID 178525261 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178518603 | HCID 178518603 | 94.1% |
Reaction Steps
(2-Amino-5-(trifluoromethyl)phenyl)(phenyl)methanone (300 mg, 1.13 mmol) and 2-(1H-tetrazol-5-yl)acetic acid (145 mg, 1.13 mmol) were suspended in ethyl acetate (10 ml). Then 1-propanephosphonic acid cyclic anhydride (2.02 g, 1.89 ml, 50% solution in EtOAc, 3.18 mmol) was added and the mixture was heated to 50° C. overnight. Then water was added at room temperature and the resulting precipitate was filtered, washed with water and heptane and dried at 50° C. and 15 mbar to afford the title compound (380 mg, 94%) as yellow solid. MS (ESI): 356.5 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09199938B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-6fbe562634c0437582afb731983155a1 |
|---|
| Source note | uspto-grants-2015_12 |
|---|